Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MUTO BRUSH

K-Number: K833330 · 1983-11-14

ApplicantMicrovasive
Decision Date1983-11-14
Product CodeFDX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MUTO BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Microvasive. It received FDA 510(k) clearance on 1983-11-14 under 510(k) number K833330. The device is classified under product code FDX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUTO BRUSH?

MUTO BRUSH is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Microvasive. The 510(k) number is K833330.

When did MUTO BRUSH receive FDA 510(k) clearance?

MUTO BRUSH received FDA 510(k) clearance on 1983-11-14, under 510(k) number K833330.

Who is the listed applicant for MUTO BRUSH?

The FDA 510(k) record lists Microvasive as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MUTO BRUSH?

The FDA product code for MUTO BRUSH is FDX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Microvasive as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K872771LOW PROFILE GASTROSTOMYK870705THERMAL COAGULATORK861323REPLACEMENT GASTROSTOMY TUBEK861309JEJUNAL FEEDING TUBEK860366CHALLENGER HOT BIOPSY FORCEPSK860589INFLATOR/DEFLATOR PISTON SYRINGE

View all 18 devices →

Related Devices (Code: FDX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250993Single Use Cytology Brush V (BC-V600P-3010)Olympus Medical Systems CorporationK220063Single Use Cytology BrushZhejiang Chuangxiang Medical Technology Co., Ltd.K192908Fusion Cytology Brush, CytoMax II Double Lumen Cytology BrushesWilson-Cook Medical, Inc.K191485Deflectable Brush Biopsy SetCook IncorporatedK182231Brush Biopsy Set ; Deflectable Brush Biopsy SetCook IncorporatedK181317Fusion Cytology Brush, CytoMax II Double Lumen Cytology BrushWilson-Cook Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑